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Journal Abstract Search

279 related items for PubMed ID: 4129973

  • 1. An inherited small extra chromosome: a mother with 46,XX,t(17;22)(pl;ql) and a son with 47,XY,+der(22)mat.
    Borgaonkar DS, McKusick VA, Farber PA.
    J Med Genet; 1973 Dec; 10(4):379-84. PubMed ID: 4129973
    [Abstract] [Full Text] [Related]

  • 2. An (11;21) translocation in four generations with chromosome 11 abnormalities in the offspring. A clinical, cytogenetical, and gene marker study.
    Jacobsen P, Hauge M, Henningsen K, Hobolth N, Mikkelsen M, Philip J.
    Hum Hered; 1973 Dec; 23(6):568-85. PubMed ID: 4134631
    [No Abstract] [Full Text] [Related]

  • 3. Segregating reciprocal (4;21) (q21;q21) translocation with proposita trisomic for parts of 4q and 21.
    De la Chapelle A, Koivisto M, Schröder J.
    J Med Genet; 1973 Dec; 10(4):384-9. PubMed ID: 4129974
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  • 4. An extra small metacentric chromosome in a mentally retarded boy.
    Ishmael J, Laurence KM.
    J Med Genet; 1968 Dec; 5(4):335-40. PubMed ID: 5713650
    [No Abstract] [Full Text] [Related]

  • 5. A new translocation between chromosomes in the 6-12 and 21-22 groups.
    Lord PM, Casey MD, Laurance BM.
    J Med Genet; 1967 Sep; 4(3):169-76. PubMed ID: 5583342
    [No Abstract] [Full Text] [Related]

  • 6. Inherited partial duplication of chromosome No. 15.
    Fujimoto A, Towner JW, Ebbin AJ, Kahlstrom EJ, Wilson MG.
    J Med Genet; 1974 Sep; 11(3):287-91. PubMed ID: 4139262
    [Abstract] [Full Text] [Related]

  • 7. Ring chromosome 18 in a patient with multiple anomalies.
    Palmer CG, Fareed N, Merritt AD.
    J Med Genet; 1967 Jun; 4(2):117-23. PubMed ID: 5619991
    [No Abstract] [Full Text] [Related]

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  • 9. Partial trisomy of 13(pter to q12) due to 47,XY, + der(13),t(13;22)(q12;q13)mat.
    Moedjono SJ, Sparkes RS.
    Hum Genet; 1979 Sep; 50(3):241-6. PubMed ID: 489007
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  • 11. A child with a ring G chromosome (46,XX, Gr).
    Nevin NC, MacLaverty B, Campbell WA.
    J Med Genet; 1971 Jun; 8(2):231-4. PubMed ID: 5096547
    [No Abstract] [Full Text] [Related]

  • 12. Case report. Familial 4-22 translocation with partial trisomy for the short arm of chromosome 4 in two sibs.
    Sartori A, Tenconi R, Baccichetti C, Pujatti G.
    Acta Paediatr Scand; 1974 Jul; 63(4):631-5. PubMed ID: 4850900
    [No Abstract] [Full Text] [Related]

  • 13. Familial C-G translocation in three relatives associated with severe mental retardation, short stature, unusual dermatoglyphics and other malformations.
    Yanagisawa S, Hiraoka K.
    J Ment Defic Res; 1971 Jun; 15(2):136-46. PubMed ID: 5559234
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  • 16. [Multiple abnormalities in a girl with a 46, XY,17q+ karyotype].
    Engel W, Reinwein H, Bombel D, Ritter H, Wolf U.
    Humangenetik; 1968 Jun; 6(4):311-25. PubMed ID: 5713617
    [No Abstract] [Full Text] [Related]

  • 17. Tertiary trisomy in a human kindred containing an E/G translocation.
    Macintyre MN, Walden DB, Hempel JM.
    Am J Hum Genet; 1971 Sep; 23(5):431-41. PubMed ID: 5092595
    [No Abstract] [Full Text] [Related]

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